Гендік және жолдық мутациялар

#1 слайд
Гендік және
жолдық мутация
Gene and genomic
mutations
1 слайд
Гендік және жолдық мутация Gene and genomic mutations
#2 слайд
Answer the questions
O1. what is larger- a gene or a chromosome?
O2. what is heredity?
O3. What is the meaning of the terms "gaploid" and
"diploid"?
O4. What could be the result of a change in the DNA
nucleotide?
O5. What is Variation?
O6. What types are variation?
O7. Fill in the square of the punnet and determine how many
genetypes and phenotyhes fre here?
2 слайд
Answer the questions O1. what is larger- a gene or a chromosome? O2. what is heredity? O3. What is the meaning of the terms "gaploid" and "diploid"? O4. What could be the result of a change in the DNA nucleotide? O5. What is Variation? O6. What types are variation? O7. Fill in the square of the punnet and determine how many genetypes and phenotyhes fre here?
#3 слайд
YOU WILL:
Determines the types and
differences of mutations
Get information about
mutagenic factors
3 слайд
YOU WILL: Determines the types and differences of mutations Get information about mutagenic factors
#4 слайд
Key terms
A gene mutation is a permanent alteration in the DNA sequence that makes up
a gene, such that the sequence differs from what is found in most people.
Genomic mutations affect not individual genes and parts of the chromosome,
but the whole genome of the cell, as a result, the number of chromosomes
changes. This type of mutation arises as a result of errors in the divergence of
chromosomes in the process of meiosis.
Chromosomal mutations is an unpredictable change that occurs in
a chromosome . These changes are most often brought on by problems that
occur during meiosis.
Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for
example a human cell having 45 or 47 chromosomes instead of the usual 46.
Polyploidy is the process of genome doubling that gives rise to organisms with multiple sets of
chromosomes.
Haploidy – reduction of a normal number jf chromosomes in 2 times when the zygote has number of
chromosomes 1n
A deletion mutation is a mistake in the DNA replication process which removes
nucleotides from the genome. A deletion mutation can remove a single nucleotide
, or entire sequences of nucleotides.
Gene duplication, a process which can result in free mutation. Chromosomal duplication,
which can cause Bloom and Rett syndrome.
Inversion-A mutation is a permanent change in the DNA sequence of a gene. Mutations in a
gene's DNA sequence can alter the amino acid sequence of the protein encoded by the gene.
Translocations -a mutations occur in chromosomes, wherein chromosomesegments change
positions. It can either take place within achromosome or between chromosomes.
4 слайд
Key terms A gene mutation is a permanent alteration in the DNA sequence that makes up a gene, such that the sequence differs from what is found in most people. Genomic mutations affect not individual genes and parts of the chromosome, but the whole genome of the cell, as a result, the number of chromosomes changes. This type of mutation arises as a result of errors in the divergence of chromosomes in the process of meiosis. Chromosomal mutations is an unpredictable change that occurs in a chromosome . These changes are most often brought on by problems that occur during meiosis. Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example a human cell having 45 or 47 chromosomes instead of the usual 46. Polyploidy is the process of genome doubling that gives rise to organisms with multiple sets of chromosomes. Haploidy – reduction of a normal number jf chromosomes in 2 times when the zygote has number of chromosomes 1n A deletion mutation is a mistake in the DNA replication process which removes nucleotides from the genome. A deletion mutation can remove a single nucleotide , or entire sequences of nucleotides. Gene duplication, a process which can result in free mutation. Chromosomal duplication, which can cause Bloom and Rett syndrome. Inversion-A mutation is a permanent change in the DNA sequence of a gene. Mutations in a gene's DNA sequence can alter the amino acid sequence of the protein encoded by the gene. Translocations -a mutations occur in chromosomes, wherein chromosomesegments change positions. It can either take place within achromosome or between chromosomes.
#5 слайд
Key terms
gene mutations- гендік мутация
Genomic mutations- геномдық мутация
Chromosomal mutations-хромосомалық м.
Aneuploidy- анеуплоидия
Polyploidy- полиплоидия
Haploidy- гаплоидия
deletion- делеция
Inversion-инверсия
Translocations- транслокация
5 слайд
Key terms gene mutations- гендік мутация Genomic mutations- геномдық мутация Chromosomal mutations-хромосомалық м. Aneuploidy- анеуплоидия Polyploidy- полиплоидия Haploidy- гаплоидия deletion- делеция Inversion-инверсия Translocations- транслокация
#6 слайд
6 слайд
#7 слайд
Жаңа сабаққа шолу
7 слайд
Жаңа сабаққа шолу
#8 слайд
Activity
8 слайд
Activity
#9 слайд
9 слайд
#10 слайд
Literacy
10 слайд
Literacy
#11 слайд
Research time
In Kazakh culture, we have a “shejire” which is pedigree
that shows seven generations. Kazakh people do not
marry if they have similarities in “Jetyata”. Make a
research and list several reasons why these individuals
cannot marry according to our traditions?
Қазақ ұлтында жеті ұрпақты бейнелейтін «шежіре»
бар. Қазақ халқы «Жеті атада» туыстық болған
жағдайда некеге тұрмайды. Зерттеу жасаңыз және
бұл адамдардың біздің дәстүрлерімізге сай некеге
тұрмауының бірнеше себептерін келтіріңіз?
11 слайд
Research time In Kazakh culture, we have a “shejire” which is pedigree that shows seven generations. Kazakh people do not marry if they have similarities in “Jetyata”. Make a research and list several reasons why these individuals cannot marry according to our traditions? Қазақ ұлтында жеті ұрпақты бейнелейтін «шежіре» бар. Қазақ халқы «Жеті атада» туыстық болған жағдайда некеге тұрмайды. Зерттеу жасаңыз және бұл адамдардың біздің дәстүрлерімізге сай некеге тұрмауының бірнеше себептерін келтіріңіз?
#12 слайд
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12 слайд
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